CO5180625A1 - 1,2,4,5-TETRAHYDRO-BENZO [D] AZEPINAS - Google Patents

1,2,4,5-TETRAHYDRO-BENZO [D] AZEPINAS

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Publication number
CO5180625A1
CO5180625A1 CO00058410A CO00058410A CO5180625A1 CO 5180625 A1 CO5180625 A1 CO 5180625A1 CO 00058410 A CO00058410 A CO 00058410A CO 00058410 A CO00058410 A CO 00058410A CO 5180625 A1 CO5180625 A1 CO 5180625A1
Authority
CO
Colombia
Prior art keywords
chr
lower alkyl
ncf3
cycloalkyl
nitro
Prior art date
Application number
CO00058410A
Other languages
Spanish (es)
Inventor
Adam Geo
Alfred Binggeli
Hans-Peter Marki
Vincent Mutel
Maurice Wilhelm
Wolfgang Wostl
Original Assignee
Hoffmann La Roche
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of CO5180625A1 publication Critical patent/CO5180625A1/en

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/10—Drugs for disorders of the urinary system of the bladder
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P21/00—Drugs for disorders of the muscular or neuromuscular system
    • A61P21/02—Muscle relaxants, e.g. for tetanus or cramps
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/08—Antiepileptics; Anticonvulsants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16—Anti-Parkinson drugs
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/22—Anxiolytics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/24—Antidepressants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • A61P25/34—Tobacco-abuse
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P3/00—Drugs for disorders of the metabolism
    • A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Abstract

La presente invención se refiere a derivados de 1,2,4,5-tetrahidro-benzo[d]azepin de la fórmula general <EMI FILE="00058410_1" ID="1" IMF=JPEG >En dondeR1 significa hidrógeno, alquilo inferior, oxígeno, halógeno, ó -OR, -O(C3-C6)cicloalquilo, -O(CHR)n-(C3-C6)cicloalquilo, -O(CHR)nCN, -O(CHR)nCF3, -O(CHR)(CHR)nNR2, -O(CHR) -(CHR)nOR, -O(CHR)n-alquenilo inferior, -OCF3, -OCF2-R, OCF2-alquenilo inferior, -OCHRF, -OCHF-alquenilo inferior, -OCF2CRF2, -OCF2Br, -O(CHR)nCF2Br -O(CHR)n-fenilo, en donde el grupo fenilo opcionalmente se puede substituir independientemente uno del otro por entre uno y tres grupos alquilo inferior, alcoxi inferior, halógeno, nitro o ciano, -O(CHR)(CHR)n-morfolino, -O(CHR)(CHR)n-pirrolidino, -O(CHR)(CHR)n-piperidino, -O(CHR)(CHR)n-imidazol, -O(CHR)(CHR)n-triazol, -O(CHR)n-piridino,-O(CHR)(CHR)n-Osi-alquilo inferior,-O(CHR)(CHR)nOS(O)2-alquilo inferior, -O(CH2)nCH=CF2, -O(CHR)n-2,2-dimetil-[1,3]dioxo-Iano, -O(CHR)n-CHOR-CH2OR, -O(CHR)n-CHOR-(CHR)n-CH2 OR o -SR o S(CHR)nCOOR, ó -NR2, -N(R)(CHR) (CHR)nOR, -N(R)(CHR)nCF3, -N(R)(CHR)(CHR)n-morfolino, -N(R)(CHR)(CHR)n-imidazol, -N(R)(CHR)(CHR)n-pirrolidino, -N(R)(CHR)(CHR)n-pirrolidin-2-ona, -N(R)(CHR)(CHR)n-piperidino, -N(R)(CHR)(CHR)n-triazol, -N(R)(CHR)n-piridino, n es 1- 6; R significa hidrógeno, alquilo inferior o alquenilo inferior, independientemente uno de otro, en el caso de que haya más de un grupo R;R2 significa nitro o ciano;R3 significa hidrógeno, alquilo inferior, =O, =S, -SR, -S(O)2-alquilo inferior, -(C3-C6)cicloalquilo o piperazino, substituido opcionalmente por alquilo inferior, o -CONR2, -(CHR)nCONR2, -(CHR)nOR, -(CH2)n-CF3, -CF3, -(CHR)nOC(O)CF3, -(CHR)nCOOR, -(CHR)nSC6H5, en donde grupo fenilo opcionalmente puede estar substituido independientemente uno de otro por entre uno y tres grupos alquilo inferior, alcoxi inferior, halógeno, nitro o ciano, -(CHR)n-1,3-dioxo-1,3-dihidro-isoindol,-(CHR)n-tetrahidro-piran-2-iloxi o -(CHR)n-S-alquilo inferior, o -NR2, NRCO-alquilo inferior, -NRCHO,-N(R)(CHR)nCN, -N(R)(CHR)nCF3, -N(R)(CHR)(CHR)n-OR, ...The present invention relates to 1,2,4,5-tetrahydro-benzo [d] azepin derivatives of the general formula <EMI FILE = "00058410_1" ID = "1" IMF = JPEG> Where R1 means hydrogen, lower alkyl , oxygen, halogen, or -OR, -O (C3-C6) cycloalkyl, -O (CHR) n- (C3-C6) cycloalkyl, -O (CHR) nCN, -O (CHR) nCF3, -O (CHR ) (CHR) nNR2, -O (CHR) - (CHR) nOR, -O (CHR) n-lower alkenyl, -OCF3, -OCF2-R, OCF2-lower alkenyl, -OCHRF, -OCHF-lower alkenyl, - OCF2CRF2, -OCF2Br, -O (CHR) nCF2Br -O (CHR) n-phenyl, wherein the phenyl group can optionally be substituted independently of one another by between one and three lower alkyl, lower alkoxy, halogen, nitro or cyano groups , -O (CHR) (CHR) n-morpholino, -O (CHR) (CHR) n-pyrrolidino, -O (CHR) (CHR) n-piperidino, -O (CHR) (CHR) n-imidazole, - O (CHR) (CHR) n-triazole, -O (CHR) n-pyridino, -O (CHR) (CHR) n-Osi-lower alkyl, -O (CHR) (CHR) nOS (O) 2-alkyl lower, -O (CH2) nCH = CF2, -O (CHR) n-2,2-dimethyl- [1,3] dioxo-ione, -O (CHR) n-CHOR-CH2OR, -O (CHR) n -CHOR- (CHR) n-CH2 OR or -SR or S (CHR) nCOOR, or -NR2, -N (R) (CHR) (CHR) nOR, -N (R) (CHR) nCF3, -N (R) (CHR) (CHR) n-morpholino, - N (R) (CHR) (CHR) n-imidazole, -N (R) (CHR) (CHR) n-pyrrolidino, -N (R) (CHR) (CHR) n-pyrrolidin-2-one, -N (R) (CHR) (CHR) n-piperidino, -N (R) (CHR) (CHR) n-triazole, -N (R) (CHR) n-pyridino, n is 1-6; R means hydrogen, lower alkyl or lower alkenyl, independently of one another, if there is more than one group R; R2 means nitro or cyano; R3 means hydrogen, lower alkyl, = O, = S, -SR, - S (O) 2-lower alkyl, - (C3-C6) cycloalkyl or piperazino, optionally substituted by lower alkyl, or -CONR2, - (CHR) nCONR2, - (CHR) nOR, - (CH2) n-CF3, - CF3, - (CHR) nOC (O) CF3, - (CHR) nCOOR, - (CHR) nSC6H5, wherein phenyl group may optionally be independently substituted from one another by between one and three lower alkyl, lower alkoxy, halogen groups, nitro or cyano, - (CHR) n-1,3-dioxo-1,3-dihydro-isoindole, - (CHR) n-tetrahydro-pyran-2-yloxy or - (CHR) nS-lower alkyl, or -NR2 , NRCO-lower alkyl, -NRCHO, -N (R) (CHR) nCN, -N (R) (CHR) nCF3, -N (R) (CHR) (CHR) n-OR, ...

CO00058410A 1999-08-06 2000-08-03 1,2,4,5-TETRAHYDRO-BENZO [D] AZEPINAS CO5180625A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP99115557 1999-08-06

Publications (1)

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CO5180625A1 true CO5180625A1 (en) 2002-07-30

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ID=8238742

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US (1) US6218385B1 (en)
JP (1) JP3260350B2 (en)
KR (1) KR100390116B1 (en)
CN (1) CN1146455C (en)
AR (1) AR025035A1 (en)
AT (1) ATE254614T1 (en)
AU (1) AU774485B2 (en)
BR (1) BR0003375A (en)
CA (1) CA2314798A1 (en)
CO (1) CO5180625A1 (en)
DE (1) DE60006618T2 (en)
ES (1) ES2209728T3 (en)
HR (1) HRP20000520A2 (en)
HU (1) HUP0003112A3 (en)
ID (1) ID26743A (en)
IL (1) IL137688A0 (en)
MA (1) MA26748A1 (en)
NO (1) NO20003966L (en)
NZ (1) NZ506096A (en)
PE (1) PE20010467A1 (en)
PL (1) PL341890A1 (en)
RU (1) RU2240317C2 (en)
SG (1) SG93251A1 (en)
TR (1) TR200002298A2 (en)
UY (1) UY26276A1 (en)
YU (1) YU49700A (en)
ZA (1) ZA200003927B (en)

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PE20010467A1 (en) 2001-04-17
DE60006618D1 (en) 2003-12-24
PL341890A1 (en) 2001-02-12
MA26748A1 (en) 2004-12-20
AU4897900A (en) 2001-02-08
KR20010082510A (en) 2001-08-30
RU2240317C2 (en) 2004-11-20
CN1283623A (en) 2001-02-14
ID26743A (en) 2001-02-08
AU774485B2 (en) 2004-07-01
YU49700A (en) 2003-04-30
IL137688A0 (en) 2001-10-31
HU0003112D0 (en) 2000-10-28
CN1146455C (en) 2004-04-21
TR200002298A3 (en) 2001-03-21
NZ506096A (en) 2002-08-28
AR025035A1 (en) 2002-11-06
ES2209728T3 (en) 2004-07-01
US6218385B1 (en) 2001-04-17
JP3260350B2 (en) 2002-02-25
NO20003966L (en) 2001-02-07
HRP20000520A2 (en) 2001-06-30
ATE254614T1 (en) 2003-12-15
CA2314798A1 (en) 2001-02-06
SG93251A1 (en) 2002-12-17
BR0003375A (en) 2001-03-13
NO20003966D0 (en) 2000-08-04
HUP0003112A3 (en) 2003-07-28
HUP0003112A2 (en) 2002-11-28
JP2001089472A (en) 2001-04-03
ZA200003927B (en) 2001-02-06
KR100390116B1 (en) 2003-07-04
TR200002298A2 (en) 2001-03-21
UY26276A1 (en) 2000-10-31
DE60006618T2 (en) 2004-09-23

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